Mechanism of Phenylurethane

Slides:



Advertisements
Similar presentations
Mass Spectrometry.
Advertisements

Organic Spectroscopy Mass Spectrometry.
Organic Mass Spectrometry Interpretation of Mass Spectra Part 3.
Chapter 14 Mass Spectroscopy.
Mass Spectrometry The substance being analyzed (solid or liquid) is injected into the mass spectrometer and vaporized at elevated temperature and reduced.
MiniQuiz 6 Answers: Which of the compounds below do you expect to absorb light in the UV-region? (circle) Hexane Ethanol Benzene Naphthalene Explain your.
Today: Brief Review of Mass Spectroscopy Discussion/Review of H-NMR, CMR Next time (our last lab lecture): Your questions Final Exam at 2:10 pm in your.
Modern techniques for structure determination of organic compounds include: Mass spectrometry Size and formula of the compound Infrared spectroscopy Functional.
Alkanes undergo extensive fragmentation
Molecular weight: Molecular ion peak M + ? odd-numbered (N...) ? isotope peaks (Cl, Br)? Alcohols … Recognize typical fragments: H 2 O, alkyl, acyl, tropylium.
Check your Unknown #3 mass spectrum
Complete this reaction equation:
Infrared Spectroscopy
Introduction to Mass Spectrometry (MS)
William H. Brown & Christopher S. Foote
Mass Spectrometry Chapter 14 Chapter 14.
12. Structure Determination: Mass Spectrometry and Infrared Spectroscopy Based on McMurry’s Organic Chemistry, 7th edition.
Introduction to Mass Spectrometry (MS)
Mass Spectrometry (MS)
Structure Determination by Spectroscopy Mass spectroscopy Ultraviolet-visible spectroscopy Infrared spectroscopy Nuclear magnetic resonance spectroscopy.
Mass Spectrometry. Atom or molecule is hit by high-energy electron Principles of Electron-Impact Mass Spectrometry e–e–e–e–
Introduction to Mass Spectrometry (MS) A mass spectrometer produces a spectrum of masses based on the structure of a molecule. The x-axis of a mass spectrum.
CH 908: Mass Spectrometry Lecture 4 Interpreting Electron Impact Mass Spectra – Continued… Recommended: Read chapters 8-9 of McLafferty Prof. Peter B.
Organic Mass Spectrometry
CHEM 344 Organic Chemistry Lab January 20 th & 21 st 2009 Structural Determination of Organic Compounds Lecture 1 – Mass Spectrometry.
Created with MindGenius Business 2005® Mass Spectrometry Mass Spectrometry.
AS 2.12 Mass spectra a. interpret fragment ion peaks in the mass spectra of simple organic compounds, eg the difference between propanal and propanone.
Mass spectrometry L.O.: Understand how fragmentation can be useful to find the molecular structure.
Mass Spectroscopy Introduction.
11 CHEM 344 Organic Chemistry Lab September 9 th and 10 th 2008 Spectroscopy of Organic Compounds Lecture 3 –Infrared and Mass Spec.
12. Structure Determination: Mass Spectrometry and Infrared Spectroscopy Based on McMurry’s Organic Chemistry, 6 th edition.
Why this Chapter? Finding structures of new molecules synthesized is critical To get a good idea of the range of structural techniques available and how.
In MS a molecule is vaporized and ionized by bombardment with a beam of high-energy electrons. E = 1600 kcal (or 70 eV). C-C BDE = 100 kcal Mass Spectrometry.
111 CHEM 344 Organic Chemistry Lab June 18 th 2008 Spectroscopy of Organic Compounds Lecture 3 –Infrared and Mass Spec Nick Hill.
CONTENTS Fragmentation of molecular ions - theory What a mass spectrum tells you Molecular ions Fragmentation Mass spectra of alkanes Mass spectra of halogenoalkanes.
Demonstrate understanding of spectroscopic data in chemistry Chemistry A.S internal credits.
Lecture 3 Mass Spectrometry and Infrared Spectroscopy.
Mass Spectrometry.
12. Structure Determination: Mass Spectrometry
Mass Spectrometry Molecular weight can be obtained from a very small sample. It does not involve the absorption or emission of light. A beam of high-energy.
Determining the Structure of an Organic Compound
FURTHER MASS SPECTROMETRY KNOCKHARDY PUBLISHING
Recognition of Molecular Ion
Chapter 15 Structure Determination by Spectroscopy (II): UV-Vis & Mass
Smt. K.R.P.Kanya Mahavidyalaya, Islampur
IR spectroscopy (review)
Determining the Structure of an Organic Compound
Introduction to Mass Spectrometry (MS)
Lecture 23 Quiz 6 Average = 72% (36 out of 50) Mass Spectrometry
Fragmentation of M+ Draw structure of M+ if possible and then draw possible heterolytic cleavages (curved arrows) or homolytic cleavages (fish hooks)
Introduction to Mass Spectrometry (MS)
Determining the Structure of an Organic Compound
Fragmentation of M+ Draw structure of M+ if possible and then draw possible heterolytic cleavages (curved arrows) or homolytic cleavages (fish hooks)
Lecture 22 Introduction to Mass Spectrometry Lecture Problem 7 Due
General Overview of the module and the methods
12. Structure Determination: Mass Spectrometry and Infrared Spectroscopy Based on McMurry’s Organic Chemistry, 7th edition.
12. Structure Determination: Mass Spectrometry and Infrared Spectroscopy Based on McMurry’s Organic Chemistry, 7th edition.
Introduction to Mass Spectrometry (MS)
12. Structure Determination: Mass Spectrometry and Infrared Spectroscopy Based on McMurry’s Organic Chemistry, 7th edition.
WM4 Instrumental analysis
Mass Spectrometry (MS)
12. Structure Determination: Mass Spectrometry and Infrared Spectroscopy Based on McMurry’s Organic Chemistry, 7th edition.
Mass Spectrometry Reading EI Spectra: Recognition of M+
Mass Spectrometry. 3 The GC-MS => A mixture of compounds is separated by gas chromatography, then identified by mass spectrometry.
In this lesson you will learn:
12. Structure Determination: Mass Spectrometry and Infrared Spectroscopy Based on McMurry’s Organic Chemistry, 7th edition.
Recognition of Molecular Ion
Recognition of Molecular Ion
Determining the Structure of an Organic Compound
Presentation transcript:

Mechanism of Phenylurethane 1-butanol and phenyl isocyanate

Mass Spectrometry Interpretation of Mass Spectra Check Mass Spectrometry Chapters in Lab and Lecture Texts Molecules of a sample are bombarded by a stream of high energy electrons Molecular ion peak M+. Molecular ion bonds break to give fragment IONS and NEUTRAL radicals or molecules. Mass Spectra only show ions, not neutrals. m/z of M+ - m/z of F+ (fragment ion) = mass of neutral Each peak can be interpreted in terms of both a fragment ion and/or a neutral loss

A Mass Spectrum tells you the molecular mass Mass Spectrometry Molecular ion peak (M+.) at m/z 32 Base peak at m/z 31 Fragment ions at 29 and 15 A Mass Spectrum tells you the molecular mass

Molecular Ion Peak: Odd or Even Mass? aniline

Isotope Peaks: 35Cl and 37Cl

Isotope Peaks: 79Br and 81Br

Molecular Ion Peak: Alcohols … 1-butanol

Favored Fragmentations The greater the stability of the fragment ion, the more intense the peak Alkyl ion stability follows carbocation chemistry rules: 3° and allyl more stable than 2° 2° more stable than 1° Acyl ions are stable (m/z 43, 57..) PhC=O+ (m/z 105…) Alpha (a) cleavage in alcohols, amines, ethers Aromatic rings do NOT fragment easily

Characteristic Fragment Ions Look for alkyl ions at m/z 43, 57, 71, 85 (14 amu or CH2 series)

Fragmentation of alkanes

Characteristic Fragment Ions Look for aryl ions at 77 (phenyl), 91 (benzyl), and 105 (benzoyl)

Fragmentation in Aromatics Tropylium Ion

Characteristic Fragment Ions Acyl ions are stable (m/z 43, 57..)

Acyl Fragment acetophenone

Characteristic Neutral Losses 15 can only be methyl 17 usually OH 18 always H2O 28 CO or CH2=CH2 29 CH3CH2 or CHO 31 CH3O 35/37 Cl (special isotope pattern too!) 42 CH2=C=O 43 CH3CO or C3H7 45 CH3CH2O or COOH 79/81 Br (special isotope pattern too!)

Weights of common fragments or neutral losses

Mass Spectrometry Summary Molecular weight: odd-numbered (N ...) ? isotope peaks (Cl, Br)? Alcohols … Recognize typical fragments: H2O, alkyl, acyl, tropylium ion …

Discussion/Review of H-NMR, CMR Next time: Bring Spectra of your Unknown #3! Brief Review of Mass Spectroscopy Discussion/Review of H-NMR, CMR